Discovery, Biological Evaluation, and Structure–Activity and −Selectivity Relationships of 6′-Substituted (<i>E</i>)-2-(Benzofuran-3(2<i>H</i>)-ylidene)-<i>N</i>-methylacetamides, a Novel Class of Potent and Selective Monoamine Oxidase Inhibitors
作者:Leonardo Pisani、Maria Barletta、Ramon Soto-Otero、Orazio Nicolotti、Estefania Mendez-Alvarez、Marco Catto、Antonellina Introcaso、Angela Stefanachi、Saverio Cellamare、Cosimo Altomare、Angelo Carotti
DOI:10.1021/jm4000769
日期:2013.3.28
The use of selective inhibitors of monoamine oxidase A (MAO-A) and B (MAO-B) holds a therapeutic relevance in the treatment of depressive disorders and Parkinson’s disease (PD), respectively. Here, the discovery of a new class of compounds acting as monoamine oxidase inhibitors (MAO-Is) and bearing a 6′-substituted (E)-2-(benzofuran-3(2H)-ylidene)-N-alkylacetamide skeleton is reported. 6′-Sulfonyloxy
使用单胺氧化酶A(MAO-A)和B(MAO-B)的选择性抑制剂分别在抑郁症和帕金森氏病(PD)的治疗中具有治疗意义。在这里,发现了一类新的充当单胺氧化酶抑制剂(MAO-Is)并带有6'-取代的(E)-2-(苯并呋喃-3(2 H)-亚烷基)-N-烷基乙酰胺骨架的化合物报告。6'-磺酰氧基衍生物表现出对MAO-A的出色亲和力(7.0 nM